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Minimum of a BS/BA is required with preference for a focus in science or biomedical discipline.
Masters degree, Advanced education and/or training/experience preferred.
Prior Experience in clinical study management or research collaborations is required
Demonstrated effectiveness in working in a multidisciplinary, matrix team situation, and demonstrated ability to manage change.
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.
Strong knowledge of Therapeutic Area(s), subject matter expertise and international experience are desirable.

Strong working knowledge of the scientific and operational issues relevant CRC to study design, drug product(s), disease characteristics, and relevant scientific and operational aspects of drug development.
Solid understanding of GCP, HCL, Regulatory, Safety, and laws applicable to CRC studies.
Comprehensive knowledge of appropriate Pfizer SOPs, processes and systems.
Good understanding of other functional areas (e.g., Clinical Supply, Finance, C&O) and organizations (e.g., RMRS, Pfizer Country Offices and Regions including U.S.)
Experience with financial and CRC drug supply forecasting.
Adept at the use of computer based tools and systems (e.g., tracking, financial, document management, etc.) used to support CRC study management (i.e. CRC system).
Excellent written and oral communication skills
Excellent project management skills; capable of managing two or more CRC asset programs at the same time
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Very useful service, easy to work with. A lot of vacancies. Regular connection with subscribers. Hope it will help me in my job search in pharma/biotech.

Olga, Physician, Pediatric Endocrinologist

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